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Journal Abstract Search

597 related items for PubMed ID: 26383224

  • 1. Reduced INF2 expression in nephrotic syndrome is possibly related to clinical severity of steroid resistance in children.
    Tamura H, Nakazato H, Kuraoka S, Yoneda K, Takahashi W, Endo F.
    Nephrology (Carlton); 2016 Jun; 21(6):467-75. PubMed ID: 26383224
    [Abstract] [Full Text] [Related]

  • 2. Synaptopodin expression in idiopathic nephrotic syndrome of childhood.
    Srivastava T, Garola RE, Whiting JM, Alon US.
    Kidney Int; 2001 Jan; 59(1):118-25. PubMed ID: 11135064
    [Abstract] [Full Text] [Related]

  • 3. Immunoexpression of podocyte-associated proteins in acquired human glomerulopathies with nephrotic syndrome.
    Wagrowska-Danilewicz M, Stasikowska O, Danilewicz M.
    Pol J Pathol; 2006 Jan; 57(1):17-21. PubMed ID: 16739878
    [Abstract] [Full Text] [Related]

  • 4. Glomerular malondialdehyde levels in patients with focal and segmental glomerulosclerosis and minimal change disease.
    Nezhad ST, Momeni B, Basiratnia M.
    Saudi J Kidney Dis Transpl; 2010 Sep; 21(5):886-91. PubMed ID: 20814126
    [Abstract] [Full Text] [Related]

  • 5. Indications for kidney biopsy in idiopathic childhood nephrotic syndrome.
    Alshami A, Roshan A, Catapang M, Jöbsis JJ, Kwok T, Polderman N, Sibley J, Sibley M, Mammen C, Matsell DG, Pediatric Nephrology Clinical Pathway Development Team.
    Pediatr Nephrol; 2017 Oct; 32(10):1897-1905. PubMed ID: 28540445
    [Abstract] [Full Text] [Related]

  • 6. Expression of DENDRIN in several glomerular diseases and correlation to pathological parameters and renal failure - preliminary study.
    Mizdrak M, Vukojević K, Filipović N, Čapkun V, Benzon B, Durdov MG.
    Diagn Pathol; 2018 Nov 20; 13(1):90. PubMed ID: 30458823
    [Abstract] [Full Text] [Related]

  • 7. Ezrin--a useful factor in the prognosis of nephrotic syndrome in children: an immunohistochemical approach.
    Ostalska-Nowicka D, Zachwieja J, Nowicki M, Kaczmarek E, Siwinska A, Witt M.
    J Clin Pathol; 2006 Sep 20; 59(9):916-20. PubMed ID: 16522749
    [Abstract] [Full Text] [Related]

  • 8. Toll-like receptor 3 (TLR-3), TLR-4 and CD80 expression in peripheral blood mononuclear cells and urinary CD80 levels in children with idiopathic nephrotic syndrome.
    Mishra OP, Kumar R, Narayan G, Srivastava P, Abhinay A, Prasad R, Singh A, Batra VV.
    Pediatr Nephrol; 2017 Aug 20; 32(8):1355-1361. PubMed ID: 28210837
    [Abstract] [Full Text] [Related]

  • 9. Immunohistochemical detection of galectin-1 in renal biopsy specimens of children and its possible role in proteinuric glomerulopathies.
    Ostalska-Nowicka D, Zachwieja J, Nowicki M, Kaczmarek E, Siwińska A, Witt M.
    Histopathology; 2007 Oct 20; 51(4):468-76. PubMed ID: 17880528
    [Abstract] [Full Text] [Related]

  • 10. Podocin and uPAR are good biomarkers in cases of Focal and segmental glomerulosclerosis in pediatric renal biopsies.
    Pereira LHM, da Silva CA, Monteiro MLGDR, Araújo LS, Rocha LP, Reis MBDR, Ramalho FS, Corrêa RRM, Silva MV, Reis MA, Machado JR.
    PLoS One; 2019 Oct 20; 14(6):e0217569. PubMed ID: 31188898
    [Abstract] [Full Text] [Related]

  • 11. [Nephrotic syndrome in minimal change disease (kidney), focal segmental glomerulosclerosis, and focal mesangioproliferative glomerulonephritis].
    Voznesenskaia TS, Sergeeva TV.
    Ter Arkh; 2002 Oct 20; 74(6):31-3. PubMed ID: 12136479
    [Abstract] [Full Text] [Related]

  • 12. Reduced podocin expression in minimal change disease and focal segmental glomerulosclerosis is related to the level of proteinuria.
    Agrawal V, Prasad N, Jain M, Pandey R.
    Clin Exp Nephrol; 2013 Dec 20; 17(6):811-8. PubMed ID: 23377573
    [Abstract] [Full Text] [Related]

  • 13. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
    Bullich G, Trujillano D, Santín S, Ossowski S, Mendizábal S, Fraga G, Madrid Á, Ariceta G, Ballarín J, Torra R, Estivill X, Ars E.
    Eur J Hum Genet; 2015 Sep 20; 23(9):1192-9. PubMed ID: 25407002
    [Abstract] [Full Text] [Related]

  • 14. In situ evaluation of podocin in normal and glomerular diseases.
    Horinouchi I, Nakazato H, Kawano T, Iyama K, Furuse A, Arizono K, Machida J, Sakamoto T, Endo F, Hattori S.
    Kidney Int; 2003 Dec 20; 64(6):2092-9. PubMed ID: 14633131
    [Abstract] [Full Text] [Related]

  • 15. INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.
    Boyer O, Nevo F, Plaisier E, Funalot B, Gribouval O, Benoit G, Huynh Cong E, Arrondel C, Tête MJ, Montjean R, Richard L, Karras A, Pouteil-Noble C, Balafrej L, Bonnardeaux A, Canaud G, Charasse C, Dantal J, Deschenes G, Deteix P, Dubourg O, Petiot P, Pouthier D, Leguern E, Guiochon-Mantel A, Broutin I, Gubler MC, Saunier S, Ronco P, Vallat JM, Alonso MA, Antignac C, Mollet G.
    N Engl J Med; 2011 Dec 22; 365(25):2377-88. PubMed ID: 22187985
    [Abstract] [Full Text] [Related]

  • 16. Glomerular Glucocorticoid Receptors Expression and Clinicopathological Types of Childhood Nephrotic Syndrome.
    Gamal Y, Badawy A, Swelam S, Tawfeek MS, Gad EF.
    Fetal Pediatr Pathol; 2017 Feb 22; 36(1):16-26. PubMed ID: 27690709
    [Abstract] [Full Text] [Related]

  • 17. Correlation of fractional excretion of magnesium with steroid responsiveness in children with nephrotic syndrome.
    Rumana J, Hanif M, Muinuddin G, Maruf-Ul-Quader M.
    Saudi J Kidney Dis Transpl; 2014 Jul 22; 25(4):830-6. PubMed ID: 24969196
    [Abstract] [Full Text] [Related]

  • 18. CD80 expression and infiltrating regulatory T cells in idiopathic nephrotic syndrome of childhood.
    Eroglu FK, Orhan D, İnözü M, Duzova A, Gulhan B, Ozaltin F, Topaloglu R.
    Pediatr Int; 2019 Dec 22; 61(12):1250-1256. PubMed ID: 31513327
    [Abstract] [Full Text] [Related]

  • 19. Serum myeloid-related protein 8/14 in minimal change- and glomerulonephritis-related nephrotic syndrome.
    Ohara S, Kawasaki Y, Maeda R, Kanno S, Suzuki Y, Suyama K, Hosoya M.
    Pediatr Int; 2016 Oct 22; 58(10):998-1002. PubMed ID: 26891373
    [Abstract] [Full Text] [Related]

  • 20. Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic.
    Safarikova M, Stekrova J, Honsova E, Horinova V, Tesar V, Reiterova J.
    BMC Med Genet; 2018 Aug 20; 19(1):147. PubMed ID: 30126379
    [Abstract] [Full Text] [Related]

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